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首页> 外文期刊>Annals of the American Thoracic Society >Using ClinicalTrials.gov to Understand the State of Clinical Research in Pulmonary, Critical Care, and Sleep Medicine
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Using ClinicalTrials.gov to Understand the State of Clinical Research in Pulmonary, Critical Care, and Sleep Medicine

机译:使用ClinicalTrials.gov了解肺,重症监护和睡眠医学的临床研究状况

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Rationale: ClinicalTrials.gov is the largest trial registry in the world. Strengthened registration requirements, including federal mandates in 2007, have increased study representation. A systematic evaluation of all registered studies has been limited by the absence of an aggregate data set and specialty-specific search terms.Objectives: We leveraged a newly transformed database containing annotated data from ClinicalTrials.gov to define the portfolio of interventional clinical research in pulmonary, critical care, and sleep medicine.Methods: Analysis was restricted to studies registered after September 2007 through September 2010 and defined as "interventional" (n = 40,970). A specialty-specific study data set (n = 2,226) was created using disease condition terms provided by data submitters and medical subject heading terms generated by a National Library of Medicine algorithm. Trial characteristics were extracted and summarized using descriptive statistics. Measurements and Main Results: Pulmonary, critical care, and sleep medicine trials composed 5.4% of all interventional studies registered over the 3-year period. In contrast, oncology and cardiovascular disease composed 21.9 and 8.4% of trials, respectively. Within pulmonary trials, asthma and chronic obstructive pulmonary disease were the most studied conditions (27.4 and 21.8% of studies, respectively), and measures of lung function or safety were the most frequent primary outcomes. Nearly two-thirds of trials indicated enrollment of 100 patients or fewer, and a majority of studies were phase II or III trials. The single largest funding source (43.5%) was industry, and study characteristics varied by funding source.
机译:理由:ClinicalTrials.gov是世界上最大的试验注册中心。增强的注册要求(包括2007年的联邦法规)增加了研究的代表性。由于缺乏汇总数据集和特定于专业的搜索词,对所有注册研究的系统评价受到了限制。目的:我们利用包含来自ClinicalTrials.gov的注释数据的新转换数据库来定义肺部介入性临床研究的产品组合方法:分析仅限于2007年9月至2010年9月之后注册的研究,定义为“介入”研究(n = 40,970)。使用由数据提交者提供的疾病条件术语和由国家医学图书馆算法生成的医学主题标题术语,创建了特定于专业的研究数据集(n = 2,226)。使用描述性统计数据提取和总结试验特征。测量和主要结果:肺,重症监护和睡眠医学试验占三年期间注册的所有干预研究的5.4%。相反,肿瘤学和心血管疾病分别占试验的21.9%和8.4%。在肺部试验中,哮喘和慢性阻塞性肺疾病是研究最多的疾病(分别为研究的27.4和21.8%),而肺功能或安全性指标是最常见的主要结局。将近三分之二的试验表明有100名或更少的患者入组,并且大多数研究为II期或III期试验。最大的资金来源(43.5%)是行业,研究特征因资金来源而异。

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